Detalhe da pesquisa
1.
Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017.
Hum Mutat
; 41(1): 212-221, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31489982
2.
A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family.
BMC Med Genet
; 21(1): 98, 2020 05 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32393189
3.
[Expert consensus on the follow-up of newborn screening for neonatal genetic and metabolic diseases].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(4): 367-372, 2020 Apr 10.
Artigo
em Zh
| MEDLINE | ID: mdl-32219815
4.
Chinese expert brief consensus on newborn screening of inherited metabolic disorders during the novel coronavirus infection epidemic.
Ann Transl Med
; 8(7): 429, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32395473